Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Valeryia, Aksianiuk"'
Autor:
Mark A Zaydman, Alexander S Little, Fidel Haro, Valeryia Aksianiuk, William J Buchser, Aaron DiAntonio, Jeffrey I Gordon, Jeffrey Milbrandt, Arjun S Raman
Publikováno v:
eLife, Vol 11 (2022)
Cellular behaviors emerge from layers of molecular interactions: proteins interact to form complexes, pathways, and phenotypes. We show that hierarchical networks of protein interactions can be defined from the statistical pattern of proteome variati
Externí odkaz:
https://doaj.org/article/b0777089e53f4af9bf100c53466b6c9d
Autor:
Mark A Zaydman, Alexander S Little, Fidel Haro, Valeryia Aksianiuk, William J Buchser, Aaron DiAntonio, Jeffrey I Gordon, Jeffrey Milbrandt, Arjun S Raman
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b3cea017ad4c8ea58d80ca9209cdd402
https://doi.org/10.7554/elife.74104.sa2
https://doi.org/10.7554/elife.74104.sa2
Publikováno v:
Medicine, science, and the law.
Mental health courts offer access to community-based care for defendants with psychiatric disorders, including posttraumatic stress disorder (PTSD). However, limited information is available on how judges make treatment decisions about evidence-based
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ce5fb681656345fe52e84abe5a621acf
https://pubmed.ncbi.nlm.nih.gov/35473423
https://pubmed.ncbi.nlm.nih.gov/35473423
Autor:
Fidel Haro, Mark A. Zaydman, William Buchser, Jeffrey Milbrandt, Valeryia Aksianiuk, Aaron DiAntonio, Arjun S. Raman, Alex G. Little, Jeffrey I. Gordon
Cellular phenotypes emerge from a hierarchy of molecular interactions: proteins interact to form complexes, pathways, and phenotypes. We show that hierarchical networks of protein interactions can be extracted from the statistical pattern of proteome
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a7db4c1c2b5afa283b45891403f689e5
https://doi.org/10.1101/2021.09.28.462107
https://doi.org/10.1101/2021.09.28.462107
Autor:
Alejandro J, Roman, Christian A, Powers, Evelyn P, Semenov, Rebecca, Sheplock, Valeryia, Aksianiuk, Robert C, Russell, Alexander, Sumaroka, Alexandra V, Garafalo, Artur V, Cideciyan, Samuel G, Jacobson
Publikováno v:
International Journal of Molecular Sciences
Recessively-inherited NR2E3 gene mutations cause an unusual retinopathy with abnormally-increased short-wavelength sensitive cone (S-cone) function, in addition to reduced rod and long/middle-wavelength sensitive cone (L/M-cone) function. Progress to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::77dc7f86d2811e5c9bf53c1a2aeeab3b
https://pubmed.ncbi.nlm.nih.gov/31117170
https://pubmed.ncbi.nlm.nih.gov/31117170
Autor:
Alexandra V. Garafalo, Alexander Sumaroka, Christian A. Powers, Samuel G. Jacobson, Alejandro J. Roman, Evelyn P. Semenov, Artur V. Cideciyan, Robert C. Russell, Rebecca Sheplock, Valeryia Aksianiuk
Publikováno v:
International Journal of Molecular Sciences, Vol 20, Iss 10, p 2497 (2019)
Recessively-inherited NR2E3 gene mutations cause an unusual retinopathy with abnormally-increased short-wavelength sensitive cone (S-cone) function, in addition to reduced rod and long/middle-wavelength sensitive cone (L/M-cone) function. Progress to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::15097d8cd7e299868ce434b07497c4a1
https://doi.org/10.3390/ijms20102497
https://doi.org/10.3390/ijms20102497